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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169167Generated: November 1, 2026

Thionyl Chloride → 4-chloro-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/1169167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(2-Chlorophenyl)propanoic acidHCID 95676—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventHeptaneHCID 8900—
Product4-chloro-2,3-dihydro-1H-inden-1-oneHCID 1133268196.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

33.5 g (181 mmol) of the 1-(2-carboxyethyl)-2-chlorobenzene and 83.4 ml of thionyl chloride are placed in a reaction vessel and stirred at 80° C. for one hour. The excess thionyl chloride is subsequently taken off and the residue is admixed with 200 ml of heptane. The reaction mixture is stirred for 30 minutes and the solvent is subsequently removed in an oil pump vacuum. The residue is taken up in 536 ml of methylene chloride and, while cooling in ice, 48.4 g (363 mmol) of aluminum trichloride are added a little at a time over a period of 10 minutes. The resulting reaction solution is stirred at 0° C. for another 2 hours before the reaction mixture is poured onto 300 ml of ice water. After the aqueous phase has been separated off and extracted once with 60 ml of toluene, the combined organic phases are washed with 80 ml of water and with 100 ml of saturated NaCl solution. After drying over magnesium sulfate, the solvent is removed in an oil pump vacuum. 29 g (96%) of the desired product are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627764B1
Source datasetuspto-grants-2003_09
ORD IDord-22c45a0048a14569a1afb2f9294c9f15
Source noteuspto-grants-2003_09